Prescription drug · ANDA
benzonatate NDC 71335-0725
Benzonatate 200 mg/1 · Capsule · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-0725-0 | 7133507250071335072500 | 6 CAPSULE in 1 BOTTLE (71335-0725-0)Marketed from May 28, 2026 | |
| 71335-0725-1 | 7133507250171335072501 | 30 CAPSULE in 1 BOTTLE (71335-0725-1)Marketed from May 28, 2026 | |
| 71335-0725-2 | 7133507250271335072502 | 100 CAPSULE in 1 BOTTLE (71335-0725-2)Marketed from May 28, 2026 | |
| 71335-0725-3 | 7133507250371335072503 | 45 CAPSULE in 1 BOTTLE (71335-0725-3)Marketed from May 28, 2026 | |
| 71335-0725-4 | 7133507250471335072504 | 20 CAPSULE in 1 BOTTLE (71335-0725-4)Marketed from May 28, 2026 | |
| 71335-0725-5 | 7133507250571335072505 | 15 CAPSULE in 1 BOTTLE (71335-0725-5)Marketed from May 28, 2026 | |
| 71335-0725-6 | 7133507250671335072506 | 21 CAPSULE in 1 BOTTLE (71335-0725-6)Marketed from May 28, 2026 | |
| 71335-0725-7 | 7133507250771335072507 | 60 CAPSULE in 1 BOTTLE (71335-0725-7)Marketed from May 28, 2026 | |
| 71335-0725-8 | 7133507250871335072508 | 50 CAPSULE in 1 BOTTLE (71335-0725-8)Marketed from May 28, 2026 | |
| 71335-0725-9 | 7133507250971335072509 | 90 CAPSULE in 1 BOTTLE (71335-0725-9)Marketed from May 28, 2026 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- benzonatate
- Generic name (nonproprietary)
- benzonatate
- Active ingredients
- Benzonatate — 200 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 040749
- Marketing start
- Listing expires
- Other FDA classes
- Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
- Identifiers
- Product ID 71335-0725_7db8b947-2c4f-4ca8-867a-bebe58f2327bSPL ID 7db8b947-2c4f-4ca8-867a-bebe58f2327bSPL set ID a788cb01-6dc3-4f28-aaa0-c23ac058c39aRxCUI 197397, 283417UNII 5P4DHS6ENR
- Pharmacologic class
- Non-narcotic Antitussive
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471335072500followed by a unit qualifier and the quantityPackage 71335-0725-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE Benzonatate USP is indicated for the symptomatic relief of cough.
Excerpt only. Read the full label for complete information.
About NDC 71335-0725
- What is NDC 71335-0725?
- 71335-0725 is the product NDC for benzonatate, Benzonatate 200 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- benzonatate.
- What is the active ingredient?
- Benzonatate.
- Who is the labeler?
- Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for benzonatate?
- 134 other product NDCs are listed under this name. See all benzonatate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other benzonatate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Benzonatate | Benzonatate 100 mg/1 | CapsuleOral | Strides Pharma Science Limited | 64380-712 | 64380-0712-0664380-0712-07 |
| Benzonatate | Benzonatate 200 mg/1 | CapsuleOral | Strides Pharma Science Limited | 64380-713 | 64380-0713-0664380-0713-07 |
| Benzonatate | Benzonatate 150 mg/1 | CapsuleOral | Anvi Pharmaceuticals Inc | 87519-111 | 87519-0111-90 |
| Benzonatate | Benzonatate 100 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-4558 | 70518-4558-0070518-4558-0170518-4558-02+1 more |
| Benzonatate | Benzonatate 100 mg/1 | CapsuleOral | Coupler LLC | 67046-1629 | 67046-1629-03 |
| Benzonatate | Benzonatate 200 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-4497 | 70518-4497-0070518-4497-01 |
| Benzonatate | Benzonatate 100 mg/1 | CapsuleOral | St. Mary's Medical Park Pharmacy | 60760-869 | 60760-0869-1560760-0869-30 |
| Benzonatate | Benzonatate 100 mg/1 | CapsuleOral | Coupler LLC | 67046-1484 | 67046-1484-03 |
| Benzonatate | Benzonatate 200 mg/1 | CapsuleOral | Direct_rx | 72189-606 | 72189-0606-2072189-0606-30 |
| Benzonatate | Benzonatate 100 mg/1 | Capsule, Liquid filledOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-898 | 23155-0898-0123155-0898-05 |
Other NDCs under ANDA 040749
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| benzonatate | Benzonatate 200 mg/1 | CapsuleOral | Proficient Rx LP | 71205-037 |
| benzonatate | Benzonatate 200 mg/1 | CapsuleOral | Proficient Rx LP | 71205-972 |